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[成人莫西拉坦的药代动力学]

[Pharmacokinetics of moxalactam in adults].

作者信息

Humbert G, Leroy A, Fillastre J P

出版信息

Sem Hop. 1983 Jun 30;59(26):1963-7.

PMID:6310787
Abstract

Specific characteristics of Moxalactam, a new beta-lactam antibiotic, are high serum concentrations, prolonged half-life and good tissular diffusion. After IM injection of a single dose of 0.25, 0.5 and 1 g, the maximum serum concentration, achieved at one hour, averages 13, 16-21 and 30-50 micrograms/ml. After rapid IV injection of 0.5 and 1 g, the average maximum serum concentrations are 90 and 150 micrograms/ml; after an IV infusion of 2 g over 20 minutes, maximum concentrations are 150 to 180 micrograms/ml. Moxalactam elimination kinetics are linear, independent from the dose and route of administration, with a distribution half-life (T 1/2 alpha) between 0.20 and 0.60 hours and an elimination half-life (T 1/2 beta) between 2 and 2.5 hours (range: 1.9 and 3.1 hours). The apparent distribution volume is between 15 and 18 liters, i.e. 20 to 25% of the body weight. Serum or total clearances and renal clearances are respectively 80 to 100 and 50 to 90 ml/mn, with wide variations from one author to another. Approximately 70 to 90% of the administered dose are eliminated in the urine over 24 hours, without any tubular secretion. Renal failure results in a progressive increase of the elimination half-life, which can reach 20 hours in patients with anuria; approximately 50% of the injected dose are recovered by hemodialysis. Many pharmacokinetic studies have demonstrated the excellent diffusion of the agent in the various tissues and body fluids, particularly in the CSF. From the collation of bacteriologic and pharmacokinetic data, dosage regimens adjusted to the renal function can be proposed.

摘要

新型β-内酰胺抗生素莫西拉酸的具体特性为血清浓度高、半衰期长且组织扩散良好。肌内注射0.25克、0.5克和1克单剂量后,1小时达到的最大血清浓度平均分别为13微克/毫升、16 - 21微克/毫升和30 - 50微克/毫升。快速静脉注射0.5克和1克后,平均最大血清浓度分别为90微克/毫升和150微克/毫升;静脉输注2克持续20分钟后,最大浓度为150至180微克/毫升。莫西拉酸的消除动力学呈线性,与剂量和给药途径无关,分布半衰期(T 1/2α)在0.20至0.60小时之间,消除半衰期(T 1/2β)在2至2.5小时之间(范围:1.9至3.1小时)。表观分布容积在15至18升之间,即体重的20%至25%。血清清除率或总清除率以及肾清除率分别为80至100毫升/分钟和50至90毫升/分钟,不同作者的数据差异较大。给药剂量的约70%至90%在24小时内从尿液中排出,无肾小管分泌。肾衰竭导致消除半衰期逐渐延长,无尿患者的消除半衰期可达20小时;约50%的注射剂量可通过血液透析回收。许多药代动力学研究表明该药物在各种组织和体液中,尤其是脑脊液中具有良好的扩散性。通过整理细菌学和药代动力学数据,可以提出根据肾功能调整的给药方案。

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